Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion> ?p ?o ?g. }
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- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion type Assertion NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_head.
- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion wasGeneratedBy ECO_0000203 NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_provenance.
- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion wasDerivedFrom befree-20140225 NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_provenance.
- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion SIO_000772 22310223 NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_provenance.
- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion evidence source_evidence_literature NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_provenance.
- NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886578.RAc1dNBxM0M_kKBg51D7GA7mL471D99ATYBU-6hVJ-hyY130_provenance.